LYSUS INFUSION SYSTEM— 510(k) K052071

Substantially Equivalent

Ekos Corp.

FDA 510(k) clearance K052071 for LYSUS INFUSION SYSTEM, Substantially Equivalent on 2005-08-16. Applicant: Ekos Corp..

Clearance details

Applicant: Ekos Corp.
Product code: Code QEY
Advisory panel: Cardiovascular
Date received: 2005-08-01
Decision date: 2005-08-16
Decision: Substantially Equivalent
Clearance type: Special
Location: Bothell, WA, US

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